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Reaction Details
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TargetHistamine H3 receptor
LigandBDBM50053275
Substrate/Competitorn/a
Meas. Tech.ChEMBL_86909 (CHEMBL698419)
Ki 5.1±n/a nM
Citation Ganellin, CRFkyerat, ABang-Andersen, BAthmani, STertiuk, WGarbarg, MLigneau, XSchwartz, JC A novel series of (phenoxyalkyl)imidazoles as potent H3-receptor histamine antagonists. J Med Chem39:3806-13 (1996) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Histamine H3 receptor
Name:Histamine H3 receptor
Synonyms:HH3R | HRH3_RAT | Hrh3
Type:G Protein-Coupled Receptor (GPCR)
Mol. Mass.:48607.98
Organism:Rattus norvegicus (rat)
Description:n/a
Residue:445
Sequence:
MERAPPDGLMNASGTLAGEAAAAGGARGFSAAWTAVLAALMALLIVATVLGNALVMLAFV
ADSSLRTQNNFFLLNLAISDFLVGAFCIPLYVPYVLTGRWTFGRGLCKLWLVVDYLLCAS
SVFNIVLISYDRFLSVTRAVSYRAQQGDTRRAVRKMALVWVLAFLLYGPAILSWEYLSGG
SSIPEGHCYAEFFYNWYFLITASTLEFFTPFLSVTFFNLSIYLNIQRRTRLRLDGGREAG
PEPPPDAQPSPPPAPPSCWGCWPKGHGEAMPLHRYGVGEAGPGVEAGEAALGGGSGGGAA
ASPTSSSGSSSRGTERPRSLKRGSKPSASSASLEKRMKMVSQSITQRFRLSRDKKVAKSL
AIIVSIFGLCWAPYTLLMIIRAACHGRCIPDYWYETSFWLLWANSAVNPVLYPLCHYSFR
RAFTKLLCPQKLKVQPHGSLEQCWK
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  Blast E-value cutoff:
BDBM50053275
n/a
NameBDBM50053275
Synonyms:4-[2-(1H-Imidazol-4-yl)-ethoxy]-benzoic acid methyl ester | CHEMBL127404
TypeSmall organic molecule
Emp. Form.C13H14N2O3
Mol. Mass.246.2619
SMILESCOC(=O)c1ccc(OCCc2cnc[nH]2)cc1
Structure
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